A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378446



Internal ID21035999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:114805446..114805823hg38UCSC Ensembl
chr4:115726602..115726979hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378446
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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